Lerche H - Search Results

1

Delirium Screening in Aphasic Patients With the Intensive Care Delirium Screening Checklist (ICDSC): A Prospective Cohort Study.

Boßelmann C, Zurloh J, Stefanou MI, Stadler V, Weber Y, Lerche H, Poli S, Ziemann U, Mengel A. Boßelmann C, et al. Among authors: lerche h. Front Neurol. 2019 Nov 12;10:1198. doi: 10.3389/fneur.2019.01198. eCollection 2019. Front Neurol. 2019. PMID: 31781026 Free PMC article.

2

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.

Weber YG, Berger A, Bebek N, Maier S, Karafyllakes S, Meyer N, Fukuyama Y, Halbach A, Hikel C, Kurlemann G, Neubauer B, Osawa M, Püst B, Rating D, Saito K, Stephani U, Tauer U, Lehmann-Horn F, Jurkat-Rott K, Lerche H. Weber YG, et al. Among authors: lerche h. Epilepsia. 2004 Jun;45(6):601-9. doi: 10.1111/j.0013-9580.2004.48203.x. Epilepsia. 2004. PMID: 15144424 Free article.

3

Ion channel defects in idiopathic epilepsies.

Lerche H, Weber YG, Jurkat-Rott K, Lehmann-Horn F. Lerche H, et al. Curr Pharm Des. 2005;11(21):2737-52. doi: 10.2174/1381612054546815. Curr Pharm Des. 2005. PMID: 16101452 Review.

4

Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain.

Weber YG, Geiger J, Kämpchen K, Landwehrmeyer B, Sommer C, Lerche H. Weber YG, et al. Among authors: lerche h. Brain Res. 2006 Mar 10;1077(1):1-6. doi: 10.1016/j.brainres.2006.01.023. Epub 2006 Feb 28. Brain Res. 2006. PMID: 16500630

5

Epileptic nystagmus: two case reports, clinical and pathophysiological review of the literature.

Weber YG, Roesche J, Lerche H. Weber YG, et al. Among authors: lerche h. J Neurol. 2006 Jun;253(6):767-71. doi: 10.1007/s00415-006-0114-2. Epub 2006 Mar 6. J Neurol. 2006. PMID: 16511649 Review.

6

Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain.

Geiger J, Weber YG, Landwehrmeyer B, Sommer C, Lerche H. Geiger J, et al. Among authors: lerche h. Neurosci Lett. 2006 May 29;400(1-2):101-4. doi: 10.1016/j.neulet.2006.02.017. Epub 2006 Mar 2. Neurosci Lett. 2006. PMID: 16513263

7

A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.

Maljevic S, Krampfl K, Cobilanschi J, Tilgen N, Beyer S, Weber YG, Schlesinger F, Ursu D, Melzer W, Cossette P, Bufler J, Lerche H, Heils A. Maljevic S, et al. Among authors: lerche h. Ann Neurol. 2006 Jun;59(6):983-7. doi: 10.1002/ana.20874. Ann Neurol. 2006. PMID: 16718694

8

A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1.

Weber YG, Jacob M, Weber G, Lerche H. Weber YG, et al. Among authors: lerche h. Epilepsia. 2008 Nov;49(11):1959-64. doi: 10.1111/j.1528-1167.2008.01646.x. Epub 2008 May 8. Epilepsia. 2008. PMID: 18479394 Free article.

9

Genetic mechanisms in idiopathic epilepsies.

Weber YG, Lerche H. Weber YG, et al. Among authors: lerche h. Dev Med Child Neurol. 2008 Sep;50(9):648-54. doi: 10.1111/j.1469-8749.2008.03058.x. Dev Med Child Neurol. 2008. PMID: 18754913 Free article. Review.

10

Cervical spinal MRI in a patient with a vagus nerve stimulator (VNS).

Roebling R, Huch K, Kassubek J, Lerche H, Weber Y. Roebling R, et al. Among authors: lerche h. Epilepsy Res. 2009 Apr;84(2-3):273-5. doi: 10.1016/j.eplepsyres.2009.02.008. Epub 2009 Mar 9. Epilepsy Res. 2009. PMID: 19269790

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